Please note that this website will be undergoing technical maintenance between 28 and 31 August. Consequently, users may experience instabilities and limited functionality. We apologise for the inconvenience.
For a better user experience please update your browser or use Chrome or Firefox browser.
Utilities
Publication detail
Home
Commission Delegated Regulation (EU) 2016/161 of 2 October 2015 supplementing Directive 2001/83/EC of the European Parliament and of the Council by laying down detailed rules for the safety features appearing on the packaging of medicinal products for human use (Text with EEA relevance)
Commission Delegated Regulation (EU) 2016/161 of 2 October 2015 supplementing Directive 2001/83/EC of the European Parliament and of the Council by laying down detailed rules for the safety features appearing on the packaging of medicinal products for human use (Text with EEA relevance)
Publication metadata
- Published:
- Corporate author(s): European Commission
- Subject: exchange of information , industrial counterfeiting , labelling , medicinal product , pharmaceutical legislation , technical specification
- OJ : JOL_2016_032_R_0001
- CELEX : 32016R0161
- IMMC : 20151002-039:C(2015)6601/822348
- PLANJO : 20151002-039
Document viewer
Note:
The publication cannot be displayed in the document viewer. Open web version
You may access it from: Download and languages